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Drug - Tagamet
The trade name of the product as shown on the labeling.

The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Cimetidine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - EQ 300MG BASE/5ML
The potency of the active ingredient(s), Cimetidine Hydrochloride. May repeat for multiple part products.

The firm name holding legal responsibility for Tagamet. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017924
The FDA assigned number to Tagamet. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Tagamet. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Approved Prior to Jan 1, 1982
The date Tagamet was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".

Reference Listed Drug (RLD) - No
The pioneer or innovator of Tagamet. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Tagamet is in. Format is RX, OTC, DISCN.

Applicant Full Name - Glaxosmithkline
The full name of the firm holding legal responsibility for the new application of Tagamet.